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Part Time Clinical Trial Operations Jobs (NOW HIRING)

IQVIA

Clinical Trial Nurse

Fargo, ND · On-site

$50 - $60/hr

Clinical Trial Nurse (Per Diem) - Fargo, ND Work Setting: Local Travel - In-Home Patient Visits Job ... It is an excellent opportunity for PRN, part-time, or experienced nurses seeking supplemental ...

Medix

Clinical Research Coordinator

Fort Worth, TX

$26 - $34/hr

Mid-July 2026 Duration: Part-time. Open ended contract. Schedule: M-F standard business hours. The ... trial operations.Contribute to the development of study-related materials and provide ...

IQVIA

Spanish Bilingual Clinical Trial Nurse

Bethesda, MD · On-site

$50 - $60/hr

Spanish Bilingual Clinical Trial Nurse - Per Diem Bethesda, MD Work Setting: Local Travel - In-Home ... It is an excellent opportunity for PRN, part-time, or experienced nurses seeking supplemental ...

New

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

... our clinical trial operations. The ideal candidate will have a strong foundation in clinical ... This is a part-time position that requires working one week per month on-site according to the ...

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Part Time Clinical Trial Operations information

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$70

How much do part time clinical trial operations jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for part time clinical trial operations in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What is the difference between Part Time Clinical Trial Operations vs Part Time Clinical Research Coordinator?

AspectPart Time Clinical Trial OperationsPart Time Clinical Research Coordinator
CredentialsTypically requires a background in healthcare, life sciences, or related certificationsRequires similar healthcare or research-related certifications, often with experience in clinical settings
Work EnvironmentWorks within clinical trial sites, hospitals, or research organizations, focusing on trial logistics and complianceWorks directly with study participants, managing data collection, consent, and study procedures
Employer & Industry UsageCommonly employed by pharmaceutical companies, CROs, and research institutionsPrimarily employed by hospitals, research centers, and academic institutions

While both roles support clinical research, Part Time Clinical Trial Operations focuses on trial logistics and compliance, whereas Part Time Clinical Research Coordinators handle participant interactions and data management. Both roles require healthcare or research certifications and are vital in the clinical trial process.

What cities are hiring for Part Time Clinical Trial Operations jobs? Cities with the most Part Time Clinical Trial Operations job openings:
What are the most commonly searched types of Clinical Trial Operations jobs? The most popular types of Clinical Trial Operations jobs are:
What states have the most Part Time Clinical Trial Operations jobs? States with the most job openings for Part Time Clinical Trial Operations jobs include:
Part Time Clinical Trial Operations jobs near you
Infographic showing various Part Time Clinical Trial Operations job openings in the United States as of August 2026, with employment types broken down into 86% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Clinical Research Coordinator (CRC)

Hawthorne Health

Springfield, MO • Hybrid

$25 - $35/hr

Part-time

Re-posted 8 days ago

Job description

About Us 
Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. Hawthorne leverages convenient, trusted, healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs. By embedding high-quality research within local communities, Hawthorne makes clinical trials more accessible and convenient for patients. Our community-based model shortens timelines and helps bring better treatments to market, faster. 
About the Position

This role is a unique opportunity for a Clinical Research Coordinator who is excited by the idea of helping build and grow one of our newer sites located in Springfield, MO. Starting as a part-time opportunity, this position has strong potential to transition into a full-time role as trial activity and patient volume continue to expand.

This opportunity is expected to average approximately 24–30 hours per week and offers a flexible mix of remote and on-site responsibilities based on clinical trial activity and site needs.

We’re looking for someone who is passionate, adaptable, and eager to make a direct impact on the site’s success and long-term growth. As the primary CRC and operational lead for the site, this individual will play a key role in overseeing and coordinating day-to-day clinical trial activities, including investigator coordination, sponsor communication, patient flow, study inventory, regulatory support, and overall site operations.

While this role offers strong ownership and leadership opportunities at the site level, you’ll also be supported by an experienced centralized operations team with expertise across patient recruitment, regulatory, quality, project management, and clinical operations to help ensure the site’s continued success and growth.

Key Responsibilities
  • Conduct and coordinate all aspects of clinical trial activities at the site.
  • Perform phlebotomy on patients, following proper clinical and safety protocols.
  • Recruit, screen, and enroll study participants according to inclusion/exclusion criteria.
  • Schedule and conduct study visits, ensuring adherence to protocol requirements.
  • Accurately collect, process, and ship biological samples per study-specific guidelines.
  • Complete and maintain study documentation, including source documents, regulatory binders, and informed consent forms.
  • Perform timely and accurate data entry into electronic data capture systems (EDC).
  • Communicate effectively with sponsors, monitors, and other research team members.
  • Ensure compliance with GCP, ICH, FDA, and IRB regulations.
  • Assist in monitoring visits and audit preparation as needed.
Qualifications
  • Minimum of 1–2 years of experience as a Clinical Research Coordinator, in a similar environment.
  • Phlebotomy certification or demonstrated competency in venipuncture (pediatric and adult required).
  • Strong understanding of clinical trial operations, regulatory documentation, and data management.
  • Excellent attention to detail, organization, and time management skills.
  • Strong interpersonal and communication abilities with patients and clinical staff.
  • Proficient in Microsoft Office and electronic data capture systems.
  • CPR certification preferred.
Hawthorne Health is transforming the clinical trial landscape through an innovative site model that integrates research into community-based settings like local pharmacies. By meeting patients where they already receive care, we are improving access, strengthening trust, and driving more inclusive and efficient trials.
 
We welcome the opportunity to connect with individuals interested in being part of this evolving model.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.To view our privacy policy and terms of use, please use the links below. Privacy Policy: https://hawthornehealth.com/privacy-policy/Terms of Use: https://hawthornehealth.com/terms-of-use/